(Q34276699)

1 August 2017

title

Hereditary sideroblastic anemia and glucose-6-phosphate dehydrogenase deficiency in a Negro family (English)

1 reference

glucose-6-phosphate dehydrogenase deficiency

1 August 2017

main subject

0 references

Hereditary sideroblastic anemia

1 reference

Prasad AS

1

1 reference

1 August 2017

Tranchida L

2

1 reference

1 August 2017

Konno ET

3

1 reference

1 August 2017

Berman L

4

1 reference

1 August 2017

Albert S

5

1 reference

1 August 2017

Sing CF

6

1 reference

1 August 2017

Brewer GJ

7

1 reference

1 August 2017

language of work or name

English

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publication date

1 June 1968

1 reference

Journal of Clinical Investigation

1 August 2017

published in

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1 August 2017

volume

47

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1 August 2017

issue

6

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1 August 2017

page(s)

1415-1424

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Studies of Glucose-6-Phosphate Dehydrogenase Activity of Individual Erythrocytes: The Methemoglobin-Elution Test for Identification of Females Heterozygous for G6PD Deficiency

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

Plasma and red cell iron turnover in normal subjects and in patients having various hematopoietic disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

Sex chromatin and gene action in the mammalian X-chromosome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

The normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

Some comments on the statistical methods used in linkage investigations.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

Gene action in the X-chromosome of the mouse (Mus musculus L.)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

Pyridoxine-responsive anemia: report of 2 cases in brothers and a review of the literature.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

The use of radioactive chromium 51 as an erythrocyte tagging agent for the determination or red cell survival in vivo

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

Familial hypochromic anaemia with hyperferricaemia. A study of two families.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=297297

Hereditary iron-loading anemia with secondary hemochromatosis

28 October 2018

1 reference

12 December 2020

Anaemia due to pyridoxine deficiency in man

1 reference

12 December 2020

Chronic refractory hypochromic anaemia with disturbed haem-metabolism

1 reference

12 December 2020

Rapid Qualitative and Quantitative Hemoglobin Fractionation: Cellulose Acetate Electrophoresis

1 reference

12 December 2020

Hemolytic anemia secondary to a familial (hereditary) defect in hemoglobin synthesis; report of a case with radioiron studies

1 reference

12 December 2020

Refractory normoblastic anaemia: a clinical and haematological study of seven cases

1 reference

12 December 2020

ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN CAUCASIANS: NEW INHERITED VARIANT

1 reference

12 December 2020

Primary or essential sideroachrestic anaemias. Pathogenesis and therapy

1 reference

12 December 2020

1 reference

12 December 2020

FAMILIAL PYRIDOXINE-RESPONSIVE ANAEMIA

1 reference

12 December 2020

The Di Guglielmo syndrome

1 reference

12 December 2020

Metabolic abnormalities of erythrocytes from patients with congenital nonspherocytic hemolytic anemia

1 reference

12 December 2020

[Hereditary leptocytic anemia in males with hemochromatosis.]

1 reference

12 December 2020

PROVEST AND BLOOD COAGULATION TESTS

1 reference

12 December 2020

Hemosiderin Estimations and Sideroblast Counts in the Differential Diagnosis of Iron Deficiency and other Anemias

1 reference

12 December 2020

Pyruvate kinase (PK) deficiency hereditary nonspherocytic hemolytic anemia

1 reference

12 December 2020

Sideroachrestic anemias

1 reference

12 December 2020

An hereditary anemia with hemochromatosis; studies of an unusual hemopathic syndrome resembling thalassemia

1 reference

12 December 2020

SIDEROBLASTS AND SIDEROBLASTIC ANAEMIA

1 reference

12 December 2020

HEREDITARY SIDEROBLASTIC ANAEMIA

1 reference

12 December 2020

Pyridoxine responsive anemia

1 reference

12 December 2020

Hypochromic anemia and hemochromatosis. Response to combined testosterone, pyridoxine, and liver extract therapy

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI105833

1 reference

1 August 2017

1 reference

1 August 2017

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